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[2014年嗜铬细胞瘤的生物学诊断]

[Biological diagnosis of pheochromocytoma in 2014].

作者信息

Rouaix-Emery Nathalie, Tierny-Fontalirand Catherine, Cardot-Bauters Catherine, Carnaille Bruno, Wemeau Jean-Louis, d'Herbomez Michèle

机构信息

Centre de biologie-pathologie-génétique, CHRU, Lille, France.

Clinique d'endocrinologie Marc Linquette, Hôpital Huriez, CHRU Lille, France.

出版信息

Ann Biol Clin (Paris). 2014 Jan-Feb;72(1):7-13. doi: 10.1684/abc.2013.0921.

Abstract

Pheochromocytomas and/or paragangliomas are rare, heterogeneous tumors of the chromaffin cells. Thirty percent of the patients presented with these diseases in a hereditary context. The biological diagnosis relies on the identification of excessive secretion of the metanephrines which are more sensitive and specific than those of catecholamines. The published recommendations give the opportunity to choose between the metanephrines in sera or urines. The concentrations of the free plasmatic metanephrines reflect the ongoing production of tumor. They are little sensitive to the renal failure. The gold standard method to measure the free metaphrines in plasma is the LC-MS/MS chromatography. This is the technical event that we use since 2008, and we relate our experience.

摘要

嗜铬细胞瘤和/或副神经节瘤是罕见的、异质性的嗜铬细胞肿瘤。30%的患者在遗传背景下出现这些疾病。生物学诊断依赖于鉴定甲氧基肾上腺素的过度分泌,其比儿茶酚胺更敏感和特异。已发表的建议提供了在血清或尿液中的甲氧基肾上腺素之间进行选择的机会。游离血浆甲氧基肾上腺素的浓度反映了肿瘤的持续产生。它们对肾衰竭不太敏感。测量血浆中游离甲氧基肾上腺素的金标准方法是液相色谱-串联质谱法(LC-MS/MS)。这是我们自2008年以来一直使用的技术方法,我们在此分享我们的经验。

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